Three-Dimensional Cell Culture Microarray for High-Throughput Studies of Stem Cell Fate

被引:73
作者
Fernandes, Tiago G. [1 ,2 ]
Kwon, Seok Joon [1 ]
Bale, Shyam Sundhar [1 ]
Lee, Moo-Yeal [3 ]
Diogo, Maria Margarida [2 ]
Clark, Douglas S. [4 ]
Cabral, Joaquim M. S. [2 ]
Dordick, Jonathan S. [1 ,5 ]
机构
[1] Rensselaer Polytech Inst, Dept Chem & Biol Engn, Ctr Biotechnol & Interdisciplinary Studies, Troy, NY 12181 USA
[2] Inst Super Tecn, Ctr Biol & Chem Engn, IBB, Lisbon, Portugal
[3] Solidus Biosci, Troy, NY USA
[4] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
[5] Rensselaer Polytech Inst, Dept Biol, Troy, NY 12180 USA
基金
美国国家卫生研究院;
关键词
stem cells; 3D cell culture; microarrays; high throughput; studies of stem cell fate; ALGINATE GEL BEADS; SELF-RENEWAL; SMALL MOLECULES; DRUG DISCOVERY; DIFFERENTIATION; EXPANSION; BIOMATERIALS; MAINTENANCE; EXPRESSION; PROTEINS;
D O I
10.1002/bit.22661
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We have developed a novel three-dimensional (3D) cellular microarray platform to enable the rapid and efficient tracking of stem cell fate and quantification of specific stem cell markers. This platform consists of a miniaturized 3D cell culture array on a functionalized glass slide for spatially addressable high-throughput screening. A microarray spotter was used to deposit cells onto a modified glass surface to yield an array consisting of cells encapsulated in alginate gel spots with volumes as low as 60 nL. A method based on an immunofluorescence technique scaled down to function on a cellular microarray was also used to quantify specific cell marker protein levels in situ. Our results revealed that this platform is suitable for studying the expansion of mouse embryonic stem (ES) cells as they retain their pluripotent and undifferentiated state. We also examined neural commitment of mouse ES cells on the microarray and observed the generation of neuroectodermal precursor cells characterized by expression of the neural marker Sox-1, whose levels were also measured in situ using a GFP reporter system. In addition, the high-throughput capacity of the platform was tested using a dual-slide system that allowed rapid screening of the effects of tretinoin and fibroblast growth factor-4 (FGF-4) on the pluripotency of mouse ES cells. This high-throughput platform is a powerful new tool for investigating cellular mechanisms involved in stem cell expansion and differentiation and provides the basis for rapid identification of signals and conditions that can be used to direct cellular responses. Biotechnol. Bioeng. 2010;106: 106-118. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:106 / 118
页数:13
相关论文
共 38 条
[1]   Biomaterial microarrays: rapid, microscale screening of polymer-cell interaction [J].
Anderson, DG ;
Putnam, D ;
Lavik, EB ;
Mahmood, TA ;
Langer, R .
BIOMATERIALS, 2005, 26 (23) :4892-4897
[2]   Nanoliter-scale synthesis of arrayed biomaterials and application to human embryonic stem cells [J].
Anderson, DG ;
Levenberg, S ;
Langer, R .
NATURE BIOTECHNOLOGY, 2004, 22 (07) :863-866
[3]   Microarrays of small molecules embedded in biodegradable polymers for use in mammalian cell-based screens [J].
Bailey, SN ;
Sabatini, DM ;
Stockwell, BR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (46) :16144-16149
[4]   Cell microarrays in drug discovery [J].
Castel, David ;
Pitaval, Amandine ;
Debily, Marie-Anne ;
Gidrol, Xavier .
DRUG DISCOVERY TODAY, 2006, 11 (13-14) :616-622
[5]   Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells [J].
Chambers, I ;
Colby, D ;
Robertson, M ;
Nichols, J ;
Lee, S ;
Tweedie, S ;
Smith, A .
CELL, 2003, 113 (05) :643-655
[6]   Spatial organization of embryonic stem cell responsiveness to autocrine gp130 ligands reveals an autoregulatory stem cell niche [J].
Davey, Ryan E. ;
Zandstra, Peter W. .
STEM CELLS, 2006, 24 (11) :2538-2548
[7]   Mimicking stem cell niches to increase stem cell expansion [J].
Dellatore, Shara M. ;
Garcia, A. Sofia ;
Miller, William M. .
CURRENT OPINION IN BIOTECHNOLOGY, 2008, 19 (05) :534-540
[8]  
Dike LE, 1999, IN VITRO CELL DEV-AN, V35, P441
[9]   Optimization and integration of expansion and neural commitment of mouse embryonic stem cells [J].
Diogo, Maria Margarida ;
Henrique, Dorningos ;
Cabral, Joaquirn M. S. .
BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2008, 49 :105-112
[10]   Matrix elasticity directs stem cell lineage specification [J].
Engler, Adam J. ;
Sen, Shamik ;
Sweeney, H. Lee ;
Discher, Dennis E. .
CELL, 2006, 126 (04) :677-689